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Details

Stereochemistry ABSOLUTE
Molecular Formula C38H54N5O9S.K
Molecular Weight 796.027
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VANIPREVIR POTASSIUM

SMILES

[K+].[H][C@]1(C[C@@H]2CN1C(=O)[C@@H](NC(=O)OCC(C)(C)CCCCC3=C4CN(CC4=CC=C3)C(=O)O2)C(C)(C)C)C(=O)N[C@@]5(C[C@H]5CC)C(=O)[N-]S(=O)(=O)C6CC6

InChI

InChIKey=GCSROPQKMQJXBI-BHHZHGTGSA-M
InChI=1S/C38H55N5O9S.K/c1-7-25-18-38(25,33(46)41-53(49,50)27-14-15-27)40-31(44)29-17-26-20-43(29)32(45)30(36(2,3)4)39-34(47)51-22-37(5,6)16-9-8-11-23-12-10-13-24-19-42(21-28(23)24)35(48)52-26;/h10,12-13,25-27,29-30H,7-9,11,14-22H2,1-6H3,(H3,39,40,41,44,46,47);/q;+1/p-1/t25-,26-,29+,30-,38-;/m1./s1

HIDE SMILES / InChI

Molecular Formula K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C38H55N5O9S
Molecular Weight 757.936
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description was created based on several sources, including http://www.rad-ar.or.jp/siori/english/kekka.cgi?n=35797 | https://www.ncbi.nlm.nih.gov/pubmed/19841155

Vaniprevir (MK-7009) is an non-covalent competitive macrocyclic inhibitor of Hepatitis C virus NS3/4A protease genotype 1a and 1b proteases at subnanomolar concentrations with modestly shifted potency against genotype 2a and 2b proteases at low nanomolar concentrations. Merck & Co. developed vaniprevir in combination with standard therapy for the twice-daily treatment of hepatitis C virus infections. The product has been launched in Japan under name VANIHEP, and Merck reported in its 2014 annual report that the product will only be available in this region.

Originator

Curator's Comment: # Merck & Co

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
VANIHEP

Approved Use

VANIHEP Capsules 150mg (Vaniprevir) indicated for the improvement of viremia in the following patients with serogroup 1 (genotype I [1a] or II [1b]) chronic hepatitis C: Patients with high levels of blood HCV RNA who are treatment-naive, or Patients who are non-responders or relapsed to therapy including interferon

Launch Date

2014
PubMed

PubMed

TitleDatePubMed
MK-7009, a potent and selective inhibitor of hepatitis C virus NS3/4A protease.
2010 Jan
Discovery of vaniprevir (MK-7009), a macrocyclic hepatitis C virus NS3/4a protease inhibitor.
2010 Mar 25
Synthesis of vaniprevir (MK-7009): lactamization to prepare a 20-membered [corrected] macrocycle.
2011 Oct 7
Synthesis of the HCV protease inhibitor Vaniprevir (MK-7009) using ring-closing metathesis strategy.
2012 Apr 20
Characterization of vaniprevir, a hepatitis C virus NS3/4A protease inhibitor, in patients with HCV genotype 1 infection: safety, antiviral activity, resistance, and pharmacokinetics.
2013 Sep
Patents

Sample Use Guides

In general, for adults 2 VANIHEP Capsules 150mg (Vaniprevir) (300 mg as the active ingredient) at a time, twice a day for 12 weeks or 24 weeks. This medicine is used in combination with peginterferon α-2b (gene recombination) and ribavirin.
Route of Administration: Oral
In a cell-based HCV replicon assay, Vaniprevir (MK-7009) showed potent activity against the genotype 1b enzyme (EC50  5 nM). In a genotype 2a replicon, the potency of MK-7009 was reduced only modestly (EC50  15 nM).
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:11:55 GMT 2023
Edited
by admin
on Fri Dec 15 17:11:55 GMT 2023
Record UNII
W0LRK0QD50
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VANIPREVIR POTASSIUM
Common Name English
VANIPREVIR POTASSIUM SALT [MI]
Common Name English
CYCLOPROPANECARBOXAMIDE, N-(((6-(2-CARBOXY-2,3-DIHYDRO-1H-ISOINDOL-4-YL)-2,2-DIMETHYLHEXYL)OXY)CARBONYL)-3-METHYL-L-VALYL-(4R)-4-HYDROXY-L-PROLYL-1-AMINO-N-(CYCLOPROPYLSULFONYL)-2-ETHYL-, (1->2)-LACTONE, POTASSIUM SALT (1:1), (1R,2R)-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID40155326
Created by admin on Fri Dec 15 17:11:55 GMT 2023 , Edited by admin on Fri Dec 15 17:11:55 GMT 2023
PRIMARY
CAS
1269195-08-5
Created by admin on Fri Dec 15 17:11:55 GMT 2023 , Edited by admin on Fri Dec 15 17:11:55 GMT 2023
PRIMARY
MERCK INDEX
m11392
Created by admin on Fri Dec 15 17:11:55 GMT 2023 , Edited by admin on Fri Dec 15 17:11:55 GMT 2023
PRIMARY Merck Index
DRUG BANK
DBSALT002107
Created by admin on Fri Dec 15 17:11:55 GMT 2023 , Edited by admin on Fri Dec 15 17:11:55 GMT 2023
PRIMARY
PUBCHEM
76956968
Created by admin on Fri Dec 15 17:11:55 GMT 2023 , Edited by admin on Fri Dec 15 17:11:55 GMT 2023
PRIMARY
FDA UNII
W0LRK0QD50
Created by admin on Fri Dec 15 17:11:55 GMT 2023 , Edited by admin on Fri Dec 15 17:11:55 GMT 2023
PRIMARY
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ACTIVE MOIETY